Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumours   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

LOC100507389 (uncharacterized LOC100507389)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100507389
Atlas_Id 66897
Location 3q23  [Link to chromosome band 3q23]
Location_base_pair Starts at 142645517 and ends at 142661378 bp from pter ( according to hg19-Feb_2009)

Note

Non-annotated gene. Preliminary data : if you are an author
who wish to write a full paper/card on this gene, go to  How to contribute

DNA/RNA

 


External links

Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)LOC100507389  100507389  uncharacterized LOC100507389
Aliases
GeneCards (Weizmann)LOC100507389
Ensembl hg19 (Hinxton)ENSG00000243818 [Gene_View]  chr3:142645517-142661378 [Contig_View]  LOC100507389 [Vega]
Ensembl hg38 (Hinxton)ENSG00000243818 [Gene_View]  chr3:142645517-142661378 [Contig_View]  LOC100507389 [Vega]
ICGC DataPortalENSG00000243818
TCGA cBioPortalLOC100507389
AceView (NCBI)LOC100507389
Genatlas (Paris)LOC100507389
WikiGenes100507389
SOURCE (Princeton)LOC100507389
Genetics Home Reference (NIH)LOC100507389
Genomic and cartography
GoldenPath hg19 (UCSC)LOC100507389  -     chr3:142645517-142661378 +  3q23   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LOC100507389  -     3q23   [Description]    (hg38-Dec_2013)
EnsemblLOC100507389 - 3q23 [CytoView hg19]  LOC100507389 - 3q23 [CytoView hg38]
Mapping of homologs : NCBILOC100507389 [Mapview hg19]  LOC100507389 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK096143 HG496120 HG496121
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000003 NC_018914 NT_005612 NW_004929311
Consensus coding sequences : CCDS (NCBI)LOC100507389
Cluster EST : UnigeneHs.38715 [ NCBI ]
CGAP (NCI)Hs.38715
Alternative Splicing GalleryENSG00000243818
Gene ExpressionLOC100507389 [ NCBI-GEO ]   LOC100507389 [ EBI - ARRAY_EXPRESS ]   LOC100507389 [ SEEK ]   LOC100507389 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100507389 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100507389
GTEX Portal (Tissue expression)LOC100507389
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100507389
DMDM Disease mutations100507389
Blocks (Seattle)LOC100507389
Human Protein AtlasENSG00000243818
Protein Interaction databases
FunCoupENSG00000243818
BioGRIDLOC100507389
STRING (EMBL)LOC100507389
ZODIACLOC100507389
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100507389
BioCentury BCIQLOC100507389
ClinGenLOC100507389
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100507389
Clinical trialLOC100507389
Miscellaneous
canSAR (ICR)LOC100507389 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100507389
EVEXLOC100507389
GoPubMedLOC100507389
iHOPLOC100507389
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Tue Mar 14 12:17:29 CET 2017

Home   Genes   Leukemias   Solid Tumours   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.